Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutations.

Laurence Faivre 1, 2 Alice Masurel-Paulet 1 Gwenaëlle Collod-Béroud 3 Bert Callewaert 4 Anne Child 5 Chantal Stheneur 6 Christine Binquet 2 Elodie Gautier 2 Bertrand Chevallier 6 Frédéric Huet 1 Bart Loeys 4, 7 Eloisa Arbustini 8 Karin Mayer 9 Mine Arslan-Kirchner 10 Anatoli Kiotsekoglou Paolo Comeglio Maurizia Grasso 8 Dorothy Halliday 11 Christophe Béroud 3 Claire Bonithon-Kopp 2 Mireille Claustres 3 Peter Robinson 12 Lesley Adès 13, 14, 15 Julie De Backer 4 Paul Coucke 4 Uta Francke 16 Anne De Paepe 4 Catherine Boileau 17, 18 Guillaume Jondeau 18, 19
Abstract : From a large series of 1009 probands with pathogenic FBN1 mutations, data for 320 patients <18 years of age at the last follow-up evaluation were analyzed (32%). At the time of diagnosis, the median age was 6.5 years. At the last examination, the population was classified as follows: neonatal Marfan syndrome, 14%; severe Marfan syndrome, 19%; classic Marfan syndrome, 32%; probable Marfan syndrome, 35%. Seventy-one percent had ascending aortic dilation, 55% ectopia lentis, and 28% major skeletal system involvement. Even when aortic complications existed in childhood, the rates of aortic surgery and aortic dissection remained low (5% and 1%, respectively). Some diagnostic features (major skeletal system involvement, striae, dural ectasia, and family history) were more frequent in the 10- to <18-year age group, whereas others (ascending aortic dilation and mitral abnormalities) were more frequent in the population with neonatal Marfan syndrome. Only 56% of children could be classified as having Marfan syndrome, according to international criteria, at their last follow-up evaluation when the presence of a FBN1 mutation was not considered as a major feature, with increasing frequency in the older age groups. Eighty-five percent of child probands fulfilled international criteria after molecular studies, which indicates that the discovery of a FBN1 mutation can be a valuable diagnostic aid in uncertain cases. The distributions of mutation types and locations in this pediatric series revealed large proportions of probands carrying mutations located in exons 24 to 32 (33%) and in-frame mutations (75%). Apart from lethal neonatal Marfan syndrome, we confirm that the majority of clinical manifestations of Marfan syndrome increase with age, which emphasizes the poor applicability of the international criteria to this diagnosis in childhood and the need for follow-up monitoring in cases of clinical suspicion of Marfan syndrome.
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Pediatrics, American Academy of Pediatrics, 2009, 123 (1), pp.391-8. 〈10.1542/peds.2008-0703〉
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Laurence Faivre, Alice Masurel-Paulet, Gwenaëlle Collod-Béroud, Bert Callewaert, Anne Child, et al.. Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutations.. Pediatrics, American Academy of Pediatrics, 2009, 123 (1), pp.391-8. 〈10.1542/peds.2008-0703〉. 〈inserm-00396263〉

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